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Distinct Embryonic Origin and Injury Response of Resident Stem Cells in Craniofacial Muscles

Craniofacial muscles emerge as a developmental novelty during the evolution from invertebrates to vertebrates, facilitating diversified modes of predation, feeding and communication. In contrast to the well-studied limb muscles, knowledge about craniofacial muscle stem cell biology has only recently...

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Autores principales: Cheng, Xu, Shi, Bing, Li, Jingtao
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281086/
https://www.ncbi.nlm.nih.gov/pubmed/34276411
http://dx.doi.org/10.3389/fphys.2021.690248
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author Cheng, Xu
Shi, Bing
Li, Jingtao
author_facet Cheng, Xu
Shi, Bing
Li, Jingtao
author_sort Cheng, Xu
collection PubMed
description Craniofacial muscles emerge as a developmental novelty during the evolution from invertebrates to vertebrates, facilitating diversified modes of predation, feeding and communication. In contrast to the well-studied limb muscles, knowledge about craniofacial muscle stem cell biology has only recently starts to be gathered. Craniofacial muscles are distinct from their counterparts in other regions in terms of both their embryonic origin and their injury response. Compared with somite-derived limb muscles, pharyngeal arch-derived craniofacial muscles demonstrate delayed myofiber reconstitution and prolonged fibrosis during repair. The regeneration of muscle is orchestrated by a blended source of stem/progenitor cells, including myogenic muscle satellite cells (MuSCs), mesenchymal fibro-adipogenic progenitors (FAPs) and other interstitial progenitors. Limb muscles host MuSCs of the Pax3 lineage, and FAPs from the mesoderm, while craniofacial muscles have MuSCs of the Mesp1 lineage and FAPs from the ectoderm-derived neural crest. Both in vivo and in vitro data revealed distinct patterns of proliferation and differentiation in these craniofacial muscle stem/progenitor cells. Additionally, the proportion of cells of different embryonic origins changes throughout postnatal development in the craniofacial muscles, creating a more dynamic niche environment than in other muscles. In-depth comparative studies of the stem cell biology of craniofacial and limb muscles might inspire the development of novel therapeutics to improve the management of myopathic diseases. Based on the most up-to-date literature, we delineated the pivotal cell populations regulating craniofacial muscle repair and identified clues that might elucidate the distinct embryonic origin and injury response in craniofacial muscle cells.
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spelling pubmed-82810862021-07-16 Distinct Embryonic Origin and Injury Response of Resident Stem Cells in Craniofacial Muscles Cheng, Xu Shi, Bing Li, Jingtao Front Physiol Physiology Craniofacial muscles emerge as a developmental novelty during the evolution from invertebrates to vertebrates, facilitating diversified modes of predation, feeding and communication. In contrast to the well-studied limb muscles, knowledge about craniofacial muscle stem cell biology has only recently starts to be gathered. Craniofacial muscles are distinct from their counterparts in other regions in terms of both their embryonic origin and their injury response. Compared with somite-derived limb muscles, pharyngeal arch-derived craniofacial muscles demonstrate delayed myofiber reconstitution and prolonged fibrosis during repair. The regeneration of muscle is orchestrated by a blended source of stem/progenitor cells, including myogenic muscle satellite cells (MuSCs), mesenchymal fibro-adipogenic progenitors (FAPs) and other interstitial progenitors. Limb muscles host MuSCs of the Pax3 lineage, and FAPs from the mesoderm, while craniofacial muscles have MuSCs of the Mesp1 lineage and FAPs from the ectoderm-derived neural crest. Both in vivo and in vitro data revealed distinct patterns of proliferation and differentiation in these craniofacial muscle stem/progenitor cells. Additionally, the proportion of cells of different embryonic origins changes throughout postnatal development in the craniofacial muscles, creating a more dynamic niche environment than in other muscles. In-depth comparative studies of the stem cell biology of craniofacial and limb muscles might inspire the development of novel therapeutics to improve the management of myopathic diseases. Based on the most up-to-date literature, we delineated the pivotal cell populations regulating craniofacial muscle repair and identified clues that might elucidate the distinct embryonic origin and injury response in craniofacial muscle cells. Frontiers Media S.A. 2021-07-01 /pmc/articles/PMC8281086/ /pubmed/34276411 http://dx.doi.org/10.3389/fphys.2021.690248 Text en Copyright © 2021 Cheng, Shi and Li. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Physiology
Cheng, Xu
Shi, Bing
Li, Jingtao
Distinct Embryonic Origin and Injury Response of Resident Stem Cells in Craniofacial Muscles
title Distinct Embryonic Origin and Injury Response of Resident Stem Cells in Craniofacial Muscles
title_full Distinct Embryonic Origin and Injury Response of Resident Stem Cells in Craniofacial Muscles
title_fullStr Distinct Embryonic Origin and Injury Response of Resident Stem Cells in Craniofacial Muscles
title_full_unstemmed Distinct Embryonic Origin and Injury Response of Resident Stem Cells in Craniofacial Muscles
title_short Distinct Embryonic Origin and Injury Response of Resident Stem Cells in Craniofacial Muscles
title_sort distinct embryonic origin and injury response of resident stem cells in craniofacial muscles
topic Physiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8281086/
https://www.ncbi.nlm.nih.gov/pubmed/34276411
http://dx.doi.org/10.3389/fphys.2021.690248
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